Dai J, Cai H R, Li Y, Meng F Q, Wu J Q
Department of Geriatrics, the First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China.
Zhonghua Jie He He Hu Xi Za Zhi. 2017 Jun 12;40(6):457-462. doi: 10.3760/cma.j.issn.1001-0939.2017.06.012.
To improve understanding of the characteristics of follicular bronchiolitis(FB). The clinical data of 3 patients with FB confirmed by thoracoscopic lung biopsy were retrospectively analyzed. A literature search was performed with "follicular bronchiolitis" as the key word in China Knowledge Resource Integrated Database, Wanfang and PubMed, Ovid Database. The time interval was from January 1947 to December 2015. Related articles of FB were retrieved and the clinical, radiographic characteristics and prognosis were analyzed. Among the 3 patients, 1 was male and 2 were female, aging 32-55 years. Two patients were asymptomatic, and 1 patient presented with fever, cough and dyspnea. Two patients showed normal pulmonary ventilatory function with decreased diffusive function, and 1 patient showed normal pulmonary function. The predominant HRCT findings were bilateral multiple small nodules and cystic opacities, patchy ground-glass opacities, reticular opacities and traction bronchiectasis. The pathological examination by thoracoscopic biopsy revealed bronchiolar and peribronchiolar lymphoid follicles. All patients were treated with corticosteroids, with 2 patients receiving immunosuppressants. Follow-up HRCT after 1-2 months showed no improvement, and further follow-up HRCT after 2-4 years revealed no change in 2 patients while the other patient had increased pulmonary nodules and cystic opacities. Seventeen articles concerning FB with complete records were included in the literature review. A total of 64 patients were reported in these articles. The typical images were bilateral multiple small nodules and ground-glass opacities, reticular opacities, and cystic opacities. The majority of patients improved after treatment of corticosteroids and (or) immunosuppressants. But our 3 cases showed no improvement. FB is a rare small airway disease which has non-specific clinical manifestations and pulmonary function. The most common imaging findings are bilateral multiple small nodules, with cystic opacities, ground-glass opacities, and reticular opacities. Surgical thoracoscopic biopsy can get ideal specimen which is useful for diagnosis. The curative effects of corticosteroids or immunosuppressants on FB need to be further clinically investigated.
为提高对滤泡性细支气管炎(FB)特征的认识,对3例经胸腔镜肺活检确诊为FB的患者的临床资料进行回顾性分析。以“滤泡性细支气管炎”为关键词,在中国知网、万方、PubMed及Ovid数据库中进行文献检索,时间跨度为1947年1月至2015年12月。检索到FB的相关文章,并对其临床、影像学特征及预后进行分析。3例患者中,男性1例,女性2例,年龄32 - 55岁。2例患者无症状,1例患者出现发热、咳嗽和呼吸困难。2例患者肺通气功能正常但弥散功能降低,1例患者肺功能正常。HRCT主要表现为双侧多发小结节及囊状阴影、斑片状磨玻璃影、网状影及牵拉性支气管扩张。胸腔镜活检病理检查显示细支气管及细支气管周围淋巴滤泡。所有患者均接受糖皮质激素治疗,2例患者加用免疫抑制剂。1 - 2个月后的随访HRCT显示无改善,2 - 4年后的进一步随访HRCT显示,2例患者无变化,另1例患者肺结节及囊状阴影增多。文献复习纳入17篇记录完整的关于FB的文章。这些文章共报道64例患者。典型影像表现为双侧多发小结节、磨玻璃影、网状影及囊状阴影。大多数患者经糖皮质激素和(或)免疫抑制剂治疗后好转,但我们的3例患者无改善。FB是一种罕见的小气道疾病,临床表现及肺功能无特异性。最常见的影像学表现为双侧多发小结节,伴有囊状阴影、磨玻璃影及网状影。胸腔镜手术活检可获得理想标本,有助于诊断。糖皮质激素或免疫抑制剂对FB的疗效有待进一步临床研究。